ADNP Brasil - Olá! Meu nome é Clarice, tenho 3 anos e fui diagnosticada com síndrome ADNP ( Helsmoortel van der Aa) quando tinha 1 ano e meio através de um exame
![Sindrome di Helsmoortel-Van der Aa: nasce l'associazione italiana dei pazienti - Osservatorio Malattie Rare Sindrome di Helsmoortel-Van der Aa: nasce l'associazione italiana dei pazienti - Osservatorio Malattie Rare](https://www.osservatoriomalattierare.it/images/stories/immagini_articoli/valentini-pascolini.jpg)
Sindrome di Helsmoortel-Van der Aa: nasce l'associazione italiana dei pazienti - Osservatorio Malattie Rare
![Clinical Presentation of a Complex Neurodevelopmental Disorder Caused by Mutations in ADNP. - Abstract - Europe PMC Clinical Presentation of a Complex Neurodevelopmental Disorder Caused by Mutations in ADNP. - Abstract - Europe PMC](https://europepmc.org/articles/PMC6139063/bin/nihms-980073-f0005.jpg)
Clinical Presentation of a Complex Neurodevelopmental Disorder Caused by Mutations in ADNP. - Abstract - Europe PMC
![Frontiers | Helsmoortel–van der Aa syndrome in a Chinese pediatric patient due to ADNP nonsense mutation: A case report Frontiers | Helsmoortel–van der Aa syndrome in a Chinese pediatric patient due to ADNP nonsense mutation: A case report](https://www.frontiersin.org/files/Articles/1122513/fped-11-1122513-HTML/image_m/fped-11-1122513-g001.jpg)
Frontiers | Helsmoortel–van der Aa syndrome in a Chinese pediatric patient due to ADNP nonsense mutation: A case report
![Helsmoortel-Van der Aa Syndrome as emerging clinical diagnosis in intellectually disabled children with autistic traits and ocular involvement - ScienceDirect Helsmoortel-Van der Aa Syndrome as emerging clinical diagnosis in intellectually disabled children with autistic traits and ocular involvement - ScienceDirect](https://ars.els-cdn.com/content/image/1-s2.0-S1090379817318615-gr1.jpg)
Helsmoortel-Van der Aa Syndrome as emerging clinical diagnosis in intellectually disabled children with autistic traits and ocular involvement - ScienceDirect
![Additional data on the clinical phenotype of Helsmoortel—Van der Aa syndrome associated with a novel truncating mutation in ADNP gene - Krajewska‐Walasek - 2016 - American Journal of Medical Genetics Part A - Additional data on the clinical phenotype of Helsmoortel—Van der Aa syndrome associated with a novel truncating mutation in ADNP gene - Krajewska‐Walasek - 2016 - American Journal of Medical Genetics Part A -](https://onlinelibrary.wiley.com/cms/asset/242bf1ed-7190-4266-a0bc-8e09986909aa/ajmga37641-fig-0001-m.jpg)
Additional data on the clinical phenotype of Helsmoortel—Van der Aa syndrome associated with a novel truncating mutation in ADNP gene - Krajewska‐Walasek - 2016 - American Journal of Medical Genetics Part A -
Meus Especiais - Chegou a vez de falar um pouquinho sobre a síndrome de Helsmoortel van der AA ou ADNP que é uma das características da minha filha mais nova, Helena! A
![IJERPH | Free Full-Text | Oro-Dental Manifestations in a Pediatric Patient Affected by Helsmoortel-Van der Aa Syndrome IJERPH | Free Full-Text | Oro-Dental Manifestations in a Pediatric Patient Affected by Helsmoortel-Van der Aa Syndrome](https://pub.mdpi-res.com/ijerph/ijerph-18-08957/article_deploy/html/images/ijerph-18-08957-g001.png?1629966477)
IJERPH | Free Full-Text | Oro-Dental Manifestations in a Pediatric Patient Affected by Helsmoortel-Van der Aa Syndrome
![Clinical Presentation of a Complex Neurodevelopmental Disorder Caused by Mutations in ADNP. - Abstract - Europe PMC Clinical Presentation of a Complex Neurodevelopmental Disorder Caused by Mutations in ADNP. - Abstract - Europe PMC](https://europepmc.org/articles/PMC6139063/bin/nihms-980073-f0004.jpg)
Clinical Presentation of a Complex Neurodevelopmental Disorder Caused by Mutations in ADNP. - Abstract - Europe PMC
![Frontal facial photographs of patients. (a–f) Patients 1 (a), 2 (b), 4... | Download Scientific Diagram Frontal facial photographs of patients. (a–f) Patients 1 (a), 2 (b), 4... | Download Scientific Diagram](https://www.researchgate.net/profile/Corrado-Romano/publication/260218887/figure/fig2/AS:278828862722052@1443489389115/Frontal-facial-photographs-of-patients-a-f-Patients-1-a-2-b-4-c-5-d-6-e_Q320.jpg)
Frontal facial photographs of patients. (a–f) Patients 1 (a), 2 (b), 4... | Download Scientific Diagram
![Frontiers | Helsmoortel–van der Aa syndrome in a Chinese pediatric patient due to ADNP nonsense mutation: A case report Frontiers | Helsmoortel–van der Aa syndrome in a Chinese pediatric patient due to ADNP nonsense mutation: A case report](https://www.frontiersin.org/files/Articles/1122513/fped-11-1122513-HTML/image_m/fped-11-1122513-g002.jpg)
Frontiers | Helsmoortel–van der Aa syndrome in a Chinese pediatric patient due to ADNP nonsense mutation: A case report
![Genes | Free Full-Text | Helsmoortel–Van der Aa Syndrome—Cardiothoracic and Ectodermal Manifestations in Two Patients as Further Support of a Previous Observation on Phenotypic Overlap with RASopathies Genes | Free Full-Text | Helsmoortel–Van der Aa Syndrome—Cardiothoracic and Ectodermal Manifestations in Two Patients as Further Support of a Previous Observation on Phenotypic Overlap with RASopathies](https://www.mdpi.com/genes/genes-13-02367/article_deploy/html/images/genes-13-02367-g001.png)
Genes | Free Full-Text | Helsmoortel–Van der Aa Syndrome—Cardiothoracic and Ectodermal Manifestations in Two Patients as Further Support of a Previous Observation on Phenotypic Overlap with RASopathies
![Sindrome di Helsmoortel-Van der Aa: un nuovo disturbo del neurosviluppo - Osservatorio Malattie Rare Sindrome di Helsmoortel-Van der Aa: un nuovo disturbo del neurosviluppo - Osservatorio Malattie Rare](https://www.osservatoriomalattierare.it/images/stories/immagini_articoli/dottssa-giulia-pascolini.jpg)
Sindrome di Helsmoortel-Van der Aa: un nuovo disturbo del neurosviluppo - Osservatorio Malattie Rare
![A heterozygous microdeletion of 20q13.13 encompassing ADNP gene in a child with Helsmoortel–van der Aa syndrome | European Journal of Human Genetics A heterozygous microdeletion of 20q13.13 encompassing ADNP gene in a child with Helsmoortel–van der Aa syndrome | European Journal of Human Genetics](https://media.springernature.com/full/springer-static/image/art%3A10.1038%2Fs41431-018-0165-8/MediaObjects/41431_2018_165_Fig1_HTML.jpg)